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Medixine Suite 9.0

by Medixine Oy EUDAMED

Withdrawn No longer placed on the EU market

Ref Medixine Suite 9.0Model Medixine Suite

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number64298300897MXSuiteT8 Basic UDI-DIDate18 Aug 2022RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Medixine Suite
Model / Reference
Medixine Suite, Medixine Suite 9.0
Primary DI / UDI-DI
06429830089704
Basic UDI-DI
64298300897MXSuiteT8
Direct Marketing DI
06429830089704
EMDN Code
Z12040182 General medicine diagnosis and monitoring instruments - software accessories
Device Class
Class IIa
Special Device Type
Software
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000002552

Other devices from Medixine Oy

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No